Fetus-in-fetu: An ususual cause for abdominal mass in infancy

Ann Surg. 1974 Jul;180(1):80-4. doi: 10.1097/00000658-197407000-00011.

Abstract

Fetus-in-fetu is an unusual cause of retroperitoneal abdominal mass in infants, which most likely arises from inclusion of a monozygotic, diamniotic twin. This entity is distinguished from teratoma by its embryological origin, its unusual location in the retroperitoneal space, its invariable benignity, and by the presence of vertebral organization with limb buds and well-developed organ systems. Diagnosis is made radiographically by the finding of a diminutive vertebral column on a plain abdominal film. The treatment of choice is total excision with special attention being given to the fetus' blood supply which may be directly from the host's superior mesenteric vessels. A well-documented example of this unusual entity that occurred in a six-week old infant male is presented.

MeSH terms

  • Abdominal Neoplasms / diagnosis*
  • Abnormalities, Severe Teratoid / diagnosis*
  • Abnormalities, Severe Teratoid / diagnostic imaging
  • Abnormalities, Severe Teratoid / genetics
  • Abnormalities, Severe Teratoid / surgery
  • Diagnosis, Differential
  • Female
  • Fetus* / diagnostic imaging
  • Fibroblasts / cytology
  • Histocompatibility Testing
  • Humans
  • Infant
  • Karyotyping
  • Male
  • Pregnancy
  • Radiography
  • Teratoma / diagnosis*
  • Twins